Ireland
--:--IST
Recruiting Not applicable

Evertor Muscle Activity as a Predictor of Achilles Tenotomy in the Management of Idiopathic Varus Equinus Clubfoot

NCT05767762 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-04-26
Last updated
2023-09-29

Condition(s) studied

Clubfoot

Investigational drug(s) / intervention(s)

scale Idiopathic Clubfoot

scale Idiopathic Clubfoot: The Dimeglo and the muscle activity scale will be performed at 3, 6 and 12 months with patient with idiopathic clubfoot

Study summary

Clubfoot is an orthopedic congenital malformation of the lower limb of the newborn evaluated by the Dimeglio score. There is a deficit of muscular balance between the agonists and antagonists to the deformity. The Dimeglio score takes into account the muscular activity but only up to one point out of 20. This study proposes to use a muscle scale inspired by the Dimeglio score to see if there is a correlation between muscle activity and the risk of tenotomy before 1 year. It will also assess the inter-examiner reproducibility of this scale.

This study is a prospective cohort study with a duration of 8 years to include about 100 feet. Infants with idiopathic Clubfoot treated with the functional method at up to 15 days of life will be included. Feet will be assessed at an inclusion visit and then at 3-6-12 months.

The primary endpoint will be the need for Achilles tenotomy before 1 year of age. The secondary endpoint will be inter-examiner reproducibility determined by statistical analysis.

The expectation of this study would be to define a predictive factor of the evolution of the PBVE in order to refine the treatment earlier.

Eligibility

Sex
ALL
Min age
0 Months
Max age
12 Months
Healthy volunteers
No
Inclusion Criteria: * idiopathic clubfoot, managed by the functional method, managed before D15 to perform the initial assessment. Exclusion Criteria: * syndromic clubfoot, management other than functional method, management after D15

Primary outcome measure(s)

  • Surgery — maximum 1 year after inclusion
    number of patient who need for Achilles tenotomy

Trial sites (1)

FacilityCityRegionStatus
Hopitaux Pediatriques de Nice Chu-Lenval Nice France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05767762 on ClinicalTrials.gov ↗ ← All trials in France